HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523735Generated: October 26, 2026
Phosphorus oxychloride → 6-Chloro-8-[5-(3-cyclobutyl-3-aza bicyclo[3.1.0]hex-6-yl)-[1,3,4]oxadiazol-2-yl]chroman-5-ylamine
https://huagongshe.com/reaction/1523735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3-Cyclobutyl-3-aza bicyclo[3.1.0]hexane-6-carboxylic acid | HCID 86724912 | — |
| Reactant | 5-Amino-6-chloro-chroman-8-carboxylic acid hydrazide | HCID 86724916 | — |
| Product | 6-Chloro-8-[5-(3-cyclobutyl-3-aza bicyclo[3.1.0]hex-6-yl)-[1,3,4]oxadiazol-2-yl]chroman-5-ylamine | HCID 71534777 | 14.1% |
Reaction Steps
To 3-cyclobutyl-3-aza bicyclo[3.1.0]hexane-6-carboxylic acid (74 mg, 0.40 mmol, obtained in preparation 8) was added phosphoryl chloride (1 mL). The mixture was stirred for 15 minutes and 5-amino-6-chloro chroman-8-carboxylic acid hydrazide (80 mg, 0.33 mmol) was added. The reaction mixture was gradually heated to reflux for 1 hour. The reaction mixture was cooled to room temperature, triturated with hexanes (2×20 mL) and the crude mass was basified with aqueous sodium bicarbonate solution. The basified mixture was extracted with 10% methanol in dichloromethane The organic layer was dried over anhydrous sodium sulphate and the solvent was removed under reduced pressure and was purified by silica gel column to obtain 6-chloro-8-[5-(3-cyclobutyl-3-aza bicyclo[3.1.0]hex-6-yl)-[1,3,4]oxadiazol-2-yl]chroman-5-yl amine (18 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09079894B2 |
|---|
| Source dataset | uspto-grants-2015_07 |
|---|
| ORD ID | ord-1aed4c554da44c39906336c9b94dc936 |
|---|
| Source note | uspto-grants-2015_07 |
|---|