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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931799Generated: October 31, 2026

Cyclopropylacetylene → (S)-2-tert-butoxy-2-(5-(4-chlorophenyl)-2-(2-cyclopropylethyl)-7-methylquinolin-6-yl)acetic acid

https://huagongshe.com/reaction/931799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylacetyleneHCID 138823—
Reactant(S)-2-tert-Butoxy-2-(5-(4-chlorophenyl)-7-methyl-2-phenethylquinolin-6-yl)acetic acidHCID 56645258—
Product(S)-2-tert-butoxy-2-(5-(4-chlorophenyl)-2-(2-cyclopropylethyl)-7-methylquinolin-6-yl)acetic acidHCID 56593456—

Reaction Steps

(S)-2-tert-Butoxy-2-(5-(4-chlorophenyl)-2-(2-cyclopropylethyl)-7-methylquinolin-6-yl)acetic acid (39) (5.7 mg) was prepared in a similar manner as compound (S)-2-tert-butoxy-2-(5-(4-chlorophenyl)-7-methyl-2-phenethylquinolin-6-yl)acetic acid of Example 37 except using ethynylcyclopropane instead of ethynylbenzene. 1H-NMR 400 MHz (CD3OD) δ 8.17 (d, J=8.4 Hz, 1 H), 7.91 (s, 1 H), 7.66 (d, J=8.8 Hz, 1 H), 7.6-7.5 (m, 3 H), 7.31 (m, 1 H), 5.18 (s, 1 H), 3.21 (m, 2 H), 2.71 (s, 3 H), 1.72 (m, 2 H), 0.92 (s, 9 H), 0.75 (m, 1 H), 0.41 (m, 2 H), 0.02 (m, 2 H); LCMS-ESI+ (m/z): [M+H]+ calcd for C27H31ClNO3: 452.2. Found: 452.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296758B2
Source datasetuspto-grants-2016_03
ORD IDord-20450a2ab72f4ea0b87a6561f0d39cf5
Source noteuspto-grants-2016_03