Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772361Generated: November 4, 2026

R-(-)-1,2-Propanediol → (1S,2R)-4'-(4-chlorophenyl)-2,2',3',9'-tetramethyl-spiro[cyclopropane-1,6'-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine]

https://huagongshe.com/reaction/1772361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantR-(-)-1,2-PropanediolHCID 259994—
ReactantRacemic 4'-(4-chlorophenyl)-2,2',3',9'-tetramethylspiro[cyclopropane-1,6'-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine]HCID 76524868—
Product(1S,2R)-4'-(4-chlorophenyl)-2,2',3',9'-tetramethyl-spiro[cyclopropane-1,6'-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine]HCID 57405267—

Reaction Steps

A procedure analogous to the scheme set forth for the synthesis of Compound 215 was followed, with the exception that (R)-propane-1,2-diol was used as starting material. LRMS (M+H)+: 383 m/z. 1H NMR (400 MHz, DMSO-d6) δ 7.50 (s, 4H), 3.80 (t, J=6.98 Hz, 1H), 2.55-2.63 (m, 3H), 2.39 (s, 3H), 1.95-2.03 (m, 1H), 1.58 (s, 3H), 1.39 (d, J=5.95 Hz, 1H), 1.05-1.12 (m, 1H), 0.79 (d, J=5.49 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249161B2
Source datasetuspto-grants-2016_02
ORD IDord-db08a1b93ad94c72a3f8697d10b70cf1
Source noteuspto-grants-2016_02