HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246793Generated: October 30, 2026
Sulfuric Acid → 1-Benzhydryl-3-isopropylaminoazetidine-3-carboxylic Acid Amide
https://huagongshe.com/reaction/1246793
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1-(Diphenylmethyl)-3-[(propan-2-yl)amino]azetidine-3-carbonitrile | HCID 21905786 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Benzhydryl-3-isopropylaminoazetidine-3-carboxylic Acid Amide | HCID 58721699 | — |
Reaction Steps
A solution of 1-benzhydryl-3-isopropylaminoazetidine-3-carbonitrile (I-(7A-106)a; 3.40 g, 11.1 mmol) in methylene chloride (25 ml) cooled in an ice bath was treated with H2SO4 (5.95 ml, 111 mmol), dropwise. After the reaction mixture was allowed to warm to room temperature and stir overnight, it was cooled in an ice bath and then carefully quenched with concentrated NH4OH to pH 11. The mixture was extracted with methylene chloride, the combined organic layers were dried (Na2SO4) and then concentrated, in vacuo, to afford a crude foam (3.3 g) that was then purified on a Biotage™ Flash 40M column using 0–2% methanol in methylene chloride as eluant to afford the title compound I-(7A-106)b (2.32 g, 64%) as a brown solid: +ESI MS (M+1) 324.4; 1H NMR (400 MHz, CD3OD) δ 7.40 (d, J=7.5 Hz, 4H), 7.24 (t, J=7.5 Hz, 4H), 7.15 (t, J=7.1 Hz, 2H), 4.46 (s, 1H), 3.53 (d, J=8.7 Hz, 2H), 3.06 (d, J=8.7 Hz, 2H), 2.90 (septuplet, J=6.4 Hz, 1H), 0.97 (d, J=6.6 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07129239B2 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-84fbbc4bc0ab4700b53ae18613874588 |
|---|
| Source note | uspto-grants-2006_10 |
|---|